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・ Tert-Amyl alcohol
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Tert-Butanesulfinamide
・ Tert-Butyl acetate
・ Tert-Butyl alcohol
・ Tert-Butyl bromide
・ Tert-Butyl chloride
・ Tert-Butyl formate
・ Tert-Butyl hydroperoxide
・ Tert-Butyl isocyanide
・ Tert-Butylamine
・ Tert-Butyldiphenylsilyl
・ Tert-Butylhydroquinone
・ Tert-Butyllithium
・ Tert-Butyloxycarbonyl protecting group
・ Tert-Butylphosphaacetylene
・ Tert-Butylthiol


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Tert-Butanesulfinamide : ウィキペディア英語版
Tert-Butanesulfinamide

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''tert''-Butanesulfinamide is an organosulfur compound and a member of the class of sulfinamides. Both enantiomeric forms are commercially available and are relevant to the asymmetric synthesis of amines as a chiral ammonia equivalent.〔Organic Syntheses, Vol. 82, p.157 (2005). (Link )〕 This methodology was introduced in 1997 by Jonathan A. Ellman.
==Synthesis==
Chiral ''tert''-butanesulfinamide can be prepared by enantioselective oxidation of inexpensive di-''tert''-butyl disulfide to the thiosulfinate followed by disulfide bond cleavage by lithium amide. In the original scope the chiral ligand used together with vanadyl acetylacetonate was prepared by condensing a chiral aminoindanol with 3,5-di-''tert''-butyl salicylaldehyde.

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